aorta dilation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the luminal space of the aorta is increased in volume or area, usually with an increase of contained fluid (Mammalian Phenotype Ontology, MP_0010574)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010574
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Genes

8 gene mutations causing the aorta dilation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP7A ATPase, Cu++ transporting, alpha polypeptide
GLA galactosidase, alpha
HBEGF heparin-binding EGF-like growth factor
KLF15 Kruppel-like factor 15
KRIT1 KRIT1, ankyrin repeat containing
MKL2 MKL/myocardin-like 2
PDGFB platelet-derived growth factor beta polypeptide
TMBIM1 transmembrane BAX inhibitor motif containing 1